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CAS 754226-40-9

:

4,4,5,5-Tetramethyl-2-[4-(phenylmethoxy)phenyl]-1,3,2-dioxaborolane

Description:
4,4,5,5-Tetramethyl-2-[4-(phenylmethoxy)phenyl]-1,3,2-dioxaborolane is an organoboron compound characterized by its dioxaborolane structure, which features a boron atom bonded to two oxygen atoms and a carbon framework. This compound contains multiple functional groups, including phenyl and methoxy substituents, which contribute to its chemical reactivity and potential applications in organic synthesis and materials science. The presence of the boron atom allows for unique reactivity, particularly in cross-coupling reactions, making it valuable in the synthesis of complex organic molecules. The tetramethyl groups enhance its solubility and stability, while the phenylmethoxy group can influence its electronic properties and interactions with other molecules. Overall, this compound is of interest in the fields of medicinal chemistry and organic electronics, where boron-containing compounds are often utilized for their distinctive properties. Its specific applications may vary based on its reactivity and the presence of substituents that can participate in further chemical transformations.
Formula:C19H23BO3
InChI:InChI=1S/C19H23BO3/c1-18(2)19(3,4)23-20(22-18)16-10-12-17(13-11-16)21-14-15-8-6-5-7-9-15/h5-13H,14H2,1-4H3
InChI key:InChIKey=KMKOKPUXZWBMEI-UHFFFAOYSA-N
SMILES:CC1(C)OB(OC1(C)C)C2=CC=C(OCC3=CC=CC=C3)C=C2
Synonyms:
  • 1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-[4-(phenylmethoxy)phenyl]-
  • 2-(4-Benzyloxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • 2-[4-(Benzyloxy)phenyl]-4,4,5,5-tetramethyl-1,3-dioxaborolane
  • 4,4,5,5-Tetramethyl-2-[4-(phenylmethoxy)phenyl]-1,3,2-dioxaborolane
  • 4-Benzyloxyphenylboronic Acid Pinacol Ester
  • 4-BenzyloxyphenylboronicAcidPinacolEster
  • 2-[4-(Benzyloxy)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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